FANCC
Compact downstream-CDS record-coverage hypothesis
| MANE transcript | ENST00000289081.8 |
|---|---|
| ClinVar P/LP records | 301 |
| Low-record-burden flag | no |
| Unit rows | 79 |
Unit-level record coverage
| Unit type | Best record coverage | Estimated payload |
|---|---|---|
| Single exon | 12.0% | 175 bp |
| Adjacent exon block | 38.9% | 599 bp |
| Downstream-CDS | 100.0% | 1,674 bp |
Why this classification?
- Downstream-CDS record coverage is 100.0% with an estimated payload of 1,674 bp (≤5 kb).
- This label is boundary-based: high coverage can occur when many coding records lie downstream of an early transcript boundary.
How to read this page
Record coverage summarizes ClinVar P/LP records mapped to this gene. It does not estimate patient coverage, editing efficiency, therapeutic efficacy, or safety.
Downstream-CDS values are transcript-boundary hypotheses. High downstream coverage can be boundary-driven and should be read with payload and context burden.
Condition-associated pathogenic-record groups
Record-level ClinVar condition facets. These are not patient cohorts, disease prevalence, or patient coverage.
| Condition label | P/LP records | Condition architecture | Local coverage | Boundary-CDS coverage |
|---|---|---|---|---|
| Fanconi anemia | 192 | Boundary-CDS payload architecture | 0.390625 | 1.000000 |
| Fanconi anemia complementation group C | 178 | Boundary-CDS payload architecture | 0.387640 | 0.983146 |
| Hereditary cancer-predisposing syndrome | 90 | Boundary-CDS payload architecture | 0.444444 | 1.000000 |